| DICER1 mutations in familial pleuropulmonary blastoma DA Hill, J Ivanovich, JR Priest, CA Gurnett, LP Dehner, D Desruisseau, ... Science 325 (5943), 965-965, 2009 | 785 | 2009 |
| Adolescent idiopathic scoliosis JC Cheng, RM Castelein, WC Chu, AJ Danielsson, MB Dobbs, TB Grivas, ... Nature reviews disease primers 1 (1), 1-21, 2015 | 693 | 2015 |
| Factors predictive of outcome after use of the Ponseti method for the treatment of idiopathic clubfeet MB Dobbs, JR Rudzki, DB Purcell, T Walton, KR Porter, CA Gurnett JBJS 86 (1), 22-27, 2004 | 653 | 2004 |
| Direct binding of G-protein βλ complex to voltage-dependent calcium channels MD Waard, H Liu, D Walker, VES Scott, CA Gurnett, KP Campbell Nature 385 (6615), 446-450, 1997 | 572 | 1997 |
| Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies HC Mefford, H Muhle, P Ostertag, S von Spiczak, K Buysse, C Baker, ... PLoS genetics 6 (5), e1000962, 2010 | 539 | 2010 |
| Update on clubfoot: etiology and treatment MB Dobbs, CA Gurnett Clinical orthopaedics and related research 467 (5), 1146-1153, 2009 | 461 | 2009 |
| Dual function of the voltage-dependent Ca2+ channel α2δ subunit in current stimulation and subunit interaction CA Gurnett, M De Waard, KP Campbell Neuron 16 (2), 431-440, 1996 | 422 | 1996 |
| A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome NA Singh, C Pappas, EJ Dahle, LRF Claes, TH Pruess, P De Jonghe, ... PLoS genetics 5 (9), e1000649, 2009 | 321 | 2009 |
| Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions HY Lee, Y Huang, N Bruneau, P Roll, EDO Roberson, M Hermann, ... Cell reports 1 (1), 2-12, 2012 | 302 | 2012 |
| Dissection of functional domains of the voltage-dependent Ca2+ channel α2δ subunit R Felix, CA Gurnett, M De Waard, KP Campbell Journal of Neuroscience 17 (18), 6884-6891, 1997 | 272 | 1997 |
| A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome AG Bassuk, RH Wallace, A Buhr, AR Buller, Z Afawi, M Shimojo, S Miyata, ... The American Journal of Human Genetics 83 (5), 572-581, 2008 | 251 | 2008 |
| Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes S Sharma, X Gao, D Londono, SE Devroy, KN Mauldin, JT Frankel, ... Human molecular genetics 20 (7), 1456-1466, 2011 | 235 | 2011 |
| Treatment of idiopathic clubfoot: an historical review MB Dobbs, JA Morcuende, CA Gurnett, IV Ponseti The Iowa orthopaedic journal 20, 59, 2000 | 225 | 2000 |
| Identification of three subunits of the high affinity ω-conotoxin MVIIC-sensitive Ca2+ channel H Liu, M De Waard, VES Scott, CA Gurnett, VA Lennon, KP Campbell Journal of Biological Chemistry 271 (23), 13804-13810, 1996 | 215 | 1996 |
| Structural and functional diversity of voltage-activated calcium channels M De Waard, CA Gurnett, KP Campbell Ion channels, 41-87, 1996 | 215 | 1996 |
| β Subunit Heterogeneity in N-type Ca2+ Channels (∗) VES Scott, M De Waard, H Liu, CA Gurnett, DP Venzke, VA Lennon, ... Journal of Biological Chemistry 271 (6), 3207-3212, 1996 | 202 | 1996 |
| BRAFV600E mutation is a negative prognosticator in pediatric ganglioglioma S Dahiya, DH Haydon, D Alvarado, CA Gurnett, DH Gutmann, JR Leonard Acta neuropathologica 125, 901-910, 2013 | 187 | 2013 |
| Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation CA Gurnett, F Alaee, LM Kruse, DM Desruisseau, JT Hecht, CA Wise, ... The American Journal of Human Genetics 83 (5), 616-622, 2008 | 185 | 2008 |
| Mutations in prickle orthologs cause seizures in flies, mice, and humans H Tao, JR Manak, L Sowers, X Mei, H Kiyonari, T Abe, NS Dahdaleh, ... The American Journal of Human Genetics 88 (2), 138-149, 2011 | 169 | 2011 |
| Extracellular interaction of the voltage-dependent Ca2+ channel α2δ and α1 subunits CA Gurnett, R Felix, KP Campbell Journal of Biological Chemistry 272 (29), 18508-18512, 1997 | 169 | 1997 |
